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Table 2 Primary and secondary outcomes for each group

From: Remimazolam-remifentanil causes less postoperative nausea and vomiting than remimazolam-alfentanil during hysteroscopy: a single-centre randomized controlled trial

 

Group RR (N = 102)

Group RA (n = 102)

p value

Primary outcome

   

 PONV n(%)

2 (2.0%)

12 (11.7%)

0.006*

Secondary outcomes

   

 Time to awakening, mean ± SD, s

200.6 ± 94.6

283.5 ± 183.1

< 0.001*

 PACU length of stay, mean ± SD, s

354.1 ± 66.8

371.8 ± 67.0

0.639

 Total remimazolam, mean ± SD, mg

22.3 ± 4.7

21.7 ± 4.5

0.722

 Adverse events, n(%)

   

  Low SpO2

15 (14.7%)

22 (21.6%)

0.203

  Bradycardia

3 (2.9%)

3 (2.9%)

1.000

  Hypotension

8 (7.8%)

10 (9.8%)

0.622

  Body movement

30 (29.4%)

27 (26.5%)

0.640

 Total remifentanil, mean ± SD, µg

69.1 ± 21.6

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  1. Note: PONV Postoperative nausea and vomiting, SD Standard deviation, PACU post anaesthesia care unit, Group RR remimazolam-remifentanil group, Group RA remimazolam-alfentanil group